Identity
HGNC
LOCATION
17p13.2
LOCUSID
ALIAS
GPCR42,GPR172B,PAR2,RBFVD,RFT1,RFVT1,hRFT1,huPAR-2
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 55065
MIM: 607883
HGNC: 30225
Ensembl: ENSG00000132517
Variants:
dbSNP: 55065
ClinVar: 55065
TCGA: ENSG00000132517
COSMIC: SLC52A1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000132517 | ENST00000254853 | Q9NWF4 |
| ENSG00000132517 | ENST00000424747 | Q9NWF4 |
| ENSG00000132517 | ENST00000512825 | F5H5Y1 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37510312 | 2023 | Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum. | 0 |
| 37510312 | 2023 | Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic Spectrum. | 0 |
| 33427755 | 2022 | Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute Pancreatitis. | 0 |
| 33427755 | 2022 | Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute Pancreatitis. | 0 |
| 34524871 | 2021 | Riboflavin transporter SLC52A1, a target of p53, suppresses cellular senescence by activating mitochondrial complex II. | 1 |
| 34524871 | 2021 | Riboflavin transporter SLC52A1, a target of p53, suppresses cellular senescence by activating mitochondrial complex II. | 1 |
| 29715086 | 2018 | The Expression of Riboflavin Transporters in Human Colorectal Cancer. | 10 |
| 30156861 | 2018 | Effect of the proinflammatory cytokine TNF-α on intestinal riboflavin uptake: inhibition mediated via transcriptional mechanism(s). | 8 |
| 29715086 | 2018 | The Expression of Riboflavin Transporters in Human Colorectal Cancer. | 10 |
| 30156861 | 2018 | Effect of the proinflammatory cytokine TNF-α on intestinal riboflavin uptake: inhibition mediated via transcriptional mechanism(s). | 8 |
| 29122468 | 2017 | An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. | 14 |
| 29122468 | 2017 | An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. | 14 |
| 25284511 | 2014 | Identification and characterization of 5'-flanking region of the human riboflavin transporter 1 gene (SLC52A1). | 3 |
| 25284511 | 2014 | Identification and characterization of 5'-flanking region of the human riboflavin transporter 1 gene (SLC52A1). | 3 |
| 23413253 | 2013 | Differentiation-dependent regulation of intestinal vitamin B(2) uptake: studies utilizing human-derived intestinal epithelial Caco-2 cells and native rat intestine. | 6 |
Citation
Dessen P
SLC52A1 (solute carrier family 52 member 1)
Atlas Genet Cytogenet Oncol Haematol. 2018-07-01
Online version: http://atlasgeneticsoncology.org/gene/57551/slc52a1-(solute-carrier-family-52-member-1)
